ES2423888T3 - Pentasacáridos de heparina sintéticos - Google Patents

Pentasacáridos de heparina sintéticos Download PDF

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Publication number
ES2423888T3
ES2423888T3 ES02766941T ES02766941T ES2423888T3 ES 2423888 T3 ES2423888 T3 ES 2423888T3 ES 02766941 T ES02766941 T ES 02766941T ES 02766941 T ES02766941 T ES 02766941T ES 2423888 T3 ES2423888 T3 ES 2423888T3
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ES
Spain
Prior art keywords
group
benzyl
substituted
groups
protecting groups
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
ES02766941T
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English (en)
Spanish (es)
Inventor
Joachim Seifert
Latika Singh
Tracie Elizabeth Ramsdale
Michael Leo West
Nicholas Barry Drinnan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Alchemia Pty Ltd
Original Assignee
Alchemia Pty Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Alchemia Pty Ltd filed Critical Alchemia Pty Ltd
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Publication of ES2423888T3 publication Critical patent/ES2423888T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H9/00—Compounds containing a hetero ring sharing at least two hetero atoms with a saccharide radical
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H11/00—Compounds containing saccharide radicals esterified by inorganic acids; Metal salts thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
    • C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
    • C07H13/04—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals attached to acyclic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
    • C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
    • C07H13/08—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals directly attached to carbocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/02—Acyclic radicals, not substituted by cyclic structures
    • C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
    • C07H15/10—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical containing unsaturated carbon-to-carbon bonds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/18—Acyclic radicals, substituted by carbocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H3/00—Compounds containing only hydrogen atoms and saccharide radicals having only carbon, hydrogen, and oxygen atoms
    • C07H3/06—Oligosaccharides, i.e. having three to five saccharide radicals attached to each other by glycosidic linkages
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
    • C07H5/04—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to nitrogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H7/00—Compounds containing non-saccharide radicals linked to saccharide radicals by a carbon-to-carbon bond
    • C07H7/02—Acyclic radicals
    • C07H7/033—Uronic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Cardiology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
ES02766941T 2001-09-07 2002-09-06 Pentasacáridos de heparina sintéticos Expired - Lifetime ES2423888T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
AUPR758701 2001-09-07
AUPR758701 2001-09-07
PCT/AU2002/001228 WO2003022860A1 (en) 2001-09-07 2002-09-06 Synthetic heparin pentasaccharides

Publications (1)

Publication Number Publication Date
ES2423888T3 true ES2423888T3 (es) 2013-09-25

Family

ID=34437858

Family Applications (1)

Application Number Title Priority Date Filing Date
ES02766941T Expired - Lifetime ES2423888T3 (es) 2001-09-07 2002-09-06 Pentasacáridos de heparina sintéticos

Country Status (10)

Country Link
US (5) US7541445B2 (ja)
EP (2) EP2557086A3 (ja)
JP (1) JP4688414B2 (ja)
CN (1) CN1558911B (ja)
AU (1) AU2002331426B2 (ja)
CA (4) CA2806604C (ja)
DK (1) DK1440077T3 (ja)
ES (1) ES2423888T3 (ja)
PT (1) PT1440077E (ja)
WO (1) WO2003022860A1 (ja)

Families Citing this family (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2423888T3 (es) * 2001-09-07 2013-09-25 Alchemia Limited Pentasacáridos de heparina sintéticos
AU2002950657A0 (en) * 2002-08-08 2002-09-12 Alchemia Limited Derivatives of monosaccharides for drug discovery
JP2006143694A (ja) * 2004-11-16 2006-06-08 Tokyo Kasei Kogyo Kk 新規ｐ−メトキシフェニル糖誘導体
ES2336297B1 (es) * 2008-10-08 2011-01-24 Laboratorios Farmaceuticos Rovi, S.A. Procedimiento de sintesis de pentasacaridos desprotegidos a partir deun pentasacarido precursos protegido.
EP2414371A4 (en) * 2009-03-30 2014-06-25 Univ Georgia HEPARANSULFATSYNTHESE
WO2011014793A2 (en) 2009-07-31 2011-02-03 Reliable Biopharmaceutical Corporation Process for preparing fondaparinux sodium and intermediates useful in the synthesis thereof
US8420790B2 (en) 2009-10-30 2013-04-16 Reliable Biopharmaceutical Corporation Efficient and scalable process for the manufacture of Fondaparinux sodium
JP6109574B2 (ja) * 2009-12-18 2017-04-05 カタラン、フランス、バインハイム、ソシエテ、アノニムＣａｔａｌｅｎｔ Ｆｒａｎｃｅ Ｂｅｉｎｈｅｉｍ Ｓａ 合成オリゴサッカリドを含有する医薬経口剤形
US9315587B2 (en) * 2011-03-10 2016-04-19 Victoria Link Limited Oligosaccharide compounds
US20130005954A1 (en) * 2011-06-28 2013-01-03 Apicore, Llc Process for preparing heparinoids and intermediates useful in the synthesis thereof
CN103360439B (zh) * 2012-04-02 2017-12-15 浙江海正药业股份有限公司 制备肝素五糖的新中间体及其制备方法
JP6138241B2 (ja) * 2012-05-25 2017-05-31 ツェジャン ハイサン ファーマシューティカル カンパニー リミテッド 完全に保護されたヘパリン五糖類およびその中間体を調製するための方法
CN102690302B (zh) * 2012-05-30 2015-07-01 济南圣泉唐和唐生物科技有限公司 1,2-O-异亚丙基-3-O-苄基-α-D-呋喃葡萄糖苷的制备方法
CN102718808A (zh) * 2012-06-04 2012-10-10 浙江星月药物科技股份有限公司 一类多糖衍生物及其中间体的制备方法
CN104619712B (zh) * 2012-06-05 2017-09-12 中央研究院 制备磺达肝素的方法和中间体
CN102775450B (zh) * 2012-07-03 2015-04-08 华东师范大学 一种1,6-脱水-2-叠氮-2-脱氧-β-D-吡喃葡萄糖的制备方法
CN102898487B (zh) * 2012-11-13 2016-03-09 麦科罗夫（南通）生物制药有限公司 一种磺达肝葵钠二糖中间体片段ba及其合成方法
CN102942601B (zh) * 2012-11-30 2015-09-30 江苏华泰晨光药业有限公司 一种磺达肝癸钠的中间体的制备方法
WO2014205115A2 (en) 2013-06-19 2014-12-24 The Regents Of The University Of California Regioselective silyl exchange of per-silylated oligosaccharides
AU2013395146A1 (en) * 2013-07-25 2016-02-18 Scinopharm Taiwan, Ltd. Process for the production of Fondaparinux sodium
US9346844B2 (en) * 2013-07-25 2016-05-24 Scinopharm Taiwan, Ltd. Process for the production of fondaparinux sodium
US10072039B2 (en) * 2013-07-25 2018-09-11 Scinopharm Taiwan, Ltd. Process for the production of Fondaparinux sodium
AU2013395144B2 (en) * 2013-07-25 2017-12-14 Scinopharm Taiwan, Ltd. Process for the production of Fondaparinux sodium
CN103601765B (zh) * 2013-09-02 2017-01-04 上海艾康睿医药科技有限公司 磺达肝癸钠及其中间体、以及制备方法
AU2014350912B2 (en) 2013-11-14 2017-07-27 Zhejiang Hisun Pharmaceutical Co., Ltd. Disaccharide intermediate and synthesis method thereof
CN104098618A (zh) * 2014-07-25 2014-10-15 河北常山生化药业股份有限公司 磺达肝癸钠中间体及其中间体和磺达肝癸钠的制备方法
WO2016040779A1 (en) * 2014-09-12 2016-03-17 The Board Of Trustees Of The University Of Illinois Urea derivatives of polyene macrolide antibiotics
US9909534B2 (en) 2014-09-22 2018-03-06 Ini Power Systems, Inc. Carbureted engine having an adjustable fuel to air ratio
CN105985387A (zh) * 2015-02-04 2016-10-05 苏州朗科生物技术有限公司 一种磺达肝癸钠杂质化合物及其制备方法和用途
CN105985388A (zh) * 2015-02-04 2016-10-05 苏州朗科生物技术有限公司 磺达肝癸钠杂质化合物及其制备方法和应用
CN104910217B (zh) * 2015-06-19 2018-04-17 天津红日药业股份有限公司 用于磺达肝癸钠质量控制的参比化合物
CN104876979B (zh) * 2015-06-19 2018-10-09 天津红日药业股份有限公司 一种具有抗Xa因子活性的磺酸化五糖化合物
US10023603B2 (en) 2015-07-16 2018-07-17 Formosa Laboratories, Inc. Preparation of monosaccharides, disaccharides, trisaccharides, and pentasaccharides of heparinoids
CN106518935B (zh) * 2016-10-26 2019-05-21 陕西国防工业职业技术学院 一种3,6-二去氧-3-氨基-l-艾杜糖及其衍生物的合成方法
CN107501359B (zh) * 2017-08-24 2020-07-31 深圳市海滨制药有限公司 一种磺达肝癸钠杂质化合物及其制备方法与应用
WO2020132625A1 (en) * 2018-12-21 2020-06-25 California Institute Of Technology Synthesis of disaccharide blocks from natural polysaccharides for heparan sulfate oligosaccharide assembly
CN109734757B (zh) * 2019-03-11 2020-09-11 淮北师范大学 一种磺达肝癸钠注射液有关物质b的制备方法
WO2021043631A1 (en) 2019-09-02 2021-03-11 Hepoligo Solutions Aps Intermediates useful for preparing iduronic acid containing di- and polysaccharides
WO2021083735A1 (en) 2019-10-29 2021-05-06 Hepoligo Solutions Aps Process for the production of 1,6-anhydro sugars
CN110746471B (zh) * 2019-11-04 2021-06-25 江苏美迪克化学品有限公司 一种磺达肝癸钠双糖中间体的制备方法
EP4247826A1 (en) * 2020-11-19 2023-09-27 Indian Institute Of Science Education And Research Silver assisted gold catalysis for the preparation of fondaparinux pentasaccharide and intermediates
CN112552359B (zh) * 2020-12-21 2022-11-25 北京大学 一种磺达肝葵钠五糖中间体自动化制备方法

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US13862A (en) * 1855-12-04 Cutting pile fabrics
US187381A (en) * 1877-02-13 Improvement in air and steasvj blowers for furnaces
US684691A (en) 1901-03-23 1901-10-15 Donald E Webster Micrometer-gage.
IL61201A (en) 1979-10-05 1984-09-30 Choay Sa Oligosaccharides having no more than 8 saccharide moieties,their obtention from heparin and pharmaceutical compositions containing them
CA1171375A (en) 1980-09-15 1984-07-24 Ulf P.F. Lindahl Oligosaccharides having selective anticoagulation activity
US4818816A (en) 1981-04-28 1989-04-04 Choay, S.A. Process for the organic synthesis of oligosaccharides and derivatives thereof
FR2519987A1 (fr) * 1982-01-15 1983-07-22 Choay Sa Trisaccharides a structures d-glucosamine, acide d-glucuronique, d-glucosamine et leur preparation
FR2504535B1 (fr) * 1981-04-28 1987-08-14 Choay Sa Disaccharides derives d'un acide uronique et d'une glucosamine et compositions pharmaceutiques les contenant pour le controle de la coagulation sanguine
FR2531436A1 (fr) * 1982-08-06 1984-02-10 Choay Sa Pentasaccharides substitues possedant des proprietes biologiques, leur preparation et leurs applications en tant que medicaments
CA1247608A (fr) 1981-12-23 1988-12-28 Jean Choay Derives a structure acide uronique, leur preparation et leurs applications biologiques
FR2518550A1 (fr) * 1981-12-23 1983-06-24 Choay Sa Procede de preparation de monosaccharides a structure acide l-iduronique
AU563351C (en) 1982-01-15 2003-06-19 Glaxo Group Limited Synthesis of oligosaccharides
FR2564468B1 (fr) 1984-05-16 1994-12-23 Choay Sa Nouveaux oligosaccharides, leur preparation par voie de synthese et leurs applications biologiques
US4801583A (en) * 1982-01-15 1989-01-31 Choay S.A. Oligosaccharides and their biological applications
JPS63218691A (ja) * 1987-03-09 1988-09-12 Rikagaku Kenkyusho 新規な５糖類化合物及びその製造法並びに抗凝血及び抗血栓剤
EP0333243A3 (en) 1988-03-10 1989-09-27 Akzo N.V. Sulphated k5 antigen and sulphated k5 antigen fragments
JPH03237101A (ja) 1989-12-18 1991-10-23 Rikagaku Kenkyusho グリコシルフォスファチジルイノシトールアンカー合成中間体及びグリコシルフォスファチジルイノシトールアンカー類縁体の合成中間体
JPH0616692A (ja) * 1992-07-03 1994-01-25 Nisshin Oil Mills Ltd:The 新規糖誘導体
CA2100821C (en) 1993-07-19 2001-01-16 Stephen Hanessian Stereocontrolled glycosidation
JP3837876B2 (ja) 1996-11-05 2006-10-25 和光純薬工業株式会社 アジドハロゲノベンジル誘導体及び水酸基の保護方法
JP3005669B2 (ja) 1996-12-19 2000-01-31 工業技術院長 不斉な含フッ素一級アミンの製造法
US6538117B1 (en) * 1999-08-10 2003-03-25 The Scripps Research Institute Programmable one-pot oligosaccharide synthesis
TWI289566B (en) * 1999-12-07 2007-11-11 N.V.Organon Antithrombotic compound
CA2435637A1 (en) 2001-01-23 2002-08-01 Massachusetts Institute Of Technology Solid- and solution -phase synthesis of heparin and other glycosaminoglycans
ES2423888T3 (es) 2001-09-07 2013-09-25 Alchemia Limited Pentasacáridos de heparina sintéticos

Also Published As

Publication number Publication date
EP2557086A3 (en) 2014-11-05
US8114970B2 (en) 2012-02-14
US20120208993A1 (en) 2012-08-16
WO2003022860A1 (en) 2003-03-20
AU2002331426A1 (en) 2003-03-24
PT1440077E (pt) 2013-06-04
DK1440077T3 (da) 2013-07-08
EP2557086A2 (en) 2013-02-13
CA2459562A1 (en) 2003-03-20
CA2806723C (en) 2015-12-29
CN1558911A (zh) 2004-12-29
US20090187013A1 (en) 2009-07-23
CA2806723A1 (en) 2003-03-20
EP1440077A1 (en) 2004-07-28
US20150005485A1 (en) 2015-01-01
JP2005505565A (ja) 2005-02-24
CA2806604A1 (en) 2003-03-20
EP1440077B1 (en) 2013-05-01
CA2459562C (en) 2013-05-07
CN1558911B (zh) 2010-05-12
CA2806561A1 (en) 2003-03-20
CA2806561C (en) 2015-12-22
US8404833B2 (en) 2013-03-26
US7541445B2 (en) 2009-06-02
AU2002331426B2 (en) 2008-01-10
US9243018B2 (en) 2016-01-26
JP4688414B2 (ja) 2011-05-25
EP1440077A4 (en) 2010-06-02
US8686131B2 (en) 2014-04-01
US20120220759A1 (en) 2012-08-30
CA2806604C (en) 2014-04-08
US20050080042A1 (en) 2005-04-14

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